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4-Bromo-2-hydroxybenzoic acid

 структура
1666-28-0
CAS №
1666-28-0
английское имя:
4-Bromo-2-hydroxybenzoic acid
Синонимы:
NSC 109120;4-BROMOSALICYLIC ACID;4-Bromosalicyclic acid;4-Bromosalicylic acid, >=98%;2-Hydroxy-4-bromobenzoicacid;4-bromo-2-hydoxybenzoic acid;4-BROMO-2-HYDROXYBENZOIC ACID;VLOOKUP(C4,[1]Export!$D:$H,5,0);Benzoicacid, 4-bromo-2-hydroxy-;4-Bromo-2-hydroxybenzoic acid 98%
CBNumber:
CB4196824
Формула:
C7H5BrO3
молекулярный вес:
217.02
MOL File:
1666-28-0.mol

4-Bromo-2-hydroxybenzoic acid атрибут

Температура плавления: 164-165°C
Температура кипения: 330.2±32.0 °C(Predicted)
плотность: 1.861±0.06 g/cm3(Predicted)
температура хранения: Keep in dark place,Inert atmosphere,Room temperature
пка: 2.71±0.10(Predicted)
форма: пудра
цвет: оранжевый
InChI: InChI=1S/C7H5BrO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,(H,10,11)
ИнЧИКей: FYAKLZKQJDBBKW-UHFFFAOYSA-N
SMILES: C(O)(=O)C1=CC=C(Br)C=C1O
Справочник по базе данных CAS: 1666-28-0(CAS DataBase Reference)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xi,Xn
Заявления о рисках 22-52/53
Заявления о безопасности 22-24/25-61
РИДАДР 2811
WGK Германия 3
Класс опасности IRRITANT
Группа упаковки
кода HS 2918290090
символ(GHS) GHS hazard pictograms
сигнальное слово Danger
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H301 Токсично при проглатывании. Острая токсичность, пероральная Категория 3 Опасность GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
Внимание
P301+P310 ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.

4-Bromo-2-hydroxybenzoic acid химические свойства, назначение, производство

Химические свойства

4-Bromo-2-hydroxybenzoic acid is a solid at normal temperature and pressure. It is stable at normal temperature and decomposes into phenol and carbon dioxide after rapid heating. It has some acidic properties.

Синтез

Under nitrogen atmosphere, add copper (II) bromide (8.8 g, 39.4 mmol, 1.2 equivalents), acetonitrile (50 ml), and 4-aminosalicylic acid (5.1 g, 49.5 mmol) to the vacuum-dried reaction flask, 1.5 equivalent). The reaction mixture was cooled to 0°C, and 2-hydroxy-4-bromobenzoic acid precursor (5.0 g, 32.6 mmol, 1.0 equiv) was added portion-wise. Additional acetonitrile (25 mL) was added to the mixture and stirred at 0 °C for 2 h. The organic extracts were combined and washed with 20% aqueous hydrochloric acid, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was dissolved in diethyl ether, and the resulting solution was extracted with 15% sodium hydroxide aqueous solution. The aqueous solution was washed with diethyl ether, acidified to pH 1 with 6N hydrochloric acid aqueous solution, and the mixture was extracted with diethyl ether. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was treated with chloroform, and the precipitate collected by filtration was 4-Bromo-2-hydroxybenzoic acid.

4-Bromo-2-hydroxybenzoic acid препаратная продукция и сырье

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